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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407044Generated: October 25, 2026

Diisopropylethylamine → Methyl 4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoro ethoxy)-1,3,5-triazin-2-ylamino)-3-fluorobenzoate

https://huagongshe.com/reaction/1407044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(4-Chlorophenyl)cyclopropanamineHCID 11344213—
ReactantMethyl 4-(4-chloro-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)-3-fluorobenzoateHCID 86691681—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoro ethoxy)-1,3,5-triazin-2-ylamino)-3-fluorobenzoateHCID 8669168095.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 4-(4-chloro-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)-3-fluorobenzoate (0.93 g, 2.45 mmol) in THF (10 mL) was added 1-(4-chlorophenyl)cyclopropanamine (0.5 g, 2.45 mmol) and Hunig's Base (1.71 mL, 9.8 mmol). The resulting mixture was refluxed at 80° C. for 16 hs. The precipitate was filtrated through a plug washing with THF to give a crude product that was purified by Biotage eluting with 4/1 to 3/2 hexane/ethyl acetate to give 1.2 g of methyl 4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoro ethoxy)-1,3,5-triazin-2-ylamino)-3-fluorobenzoate as product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916702B2
Source datasetuspto-grants-2014_12
ORD IDord-564a4d779d1e407fb0f3e388592d3a21
Source noteuspto-grants-2014_12